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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >RECENT PROGRESS OF NEW CATALYTIC SYNTHETIC METHODS FOR NITROGEN HETEROCYCLES BASED ON HYDROGEN TRANSFER REACTIONS
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RECENT PROGRESS OF NEW CATALYTIC SYNTHETIC METHODS FOR NITROGEN HETEROCYCLES BASED ON HYDROGEN TRANSFER REACTIONS

机译:基于氢转移反应的氮杂环催化合成新方法的最新进展

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摘要

This review summarizes a variety of synthetic methods for nitrogen heterocycles based on hydrogen transfer reactions catalyzed by transition metals in a past decade. Most of them employ iridium and ruthenium complexes as the catalysts and provide a versatile and environmentally benign synthetic methodology of various nitrogen heterocyclic compounds. Intermolecular cyclization reactions of amines with alcohols afford 5-7 membered alicyclic amines, quinolines, piperazines, indoles, quinoxalines, pyrroles, benzimidazoles, and benzoxazoles. Intramolecular cyclization reactions of amino alcohols give indoles, 1,2,3,4-tetrahydroqunolines, 1,2,3,4-tetrahydroquinoxalines, 3,4-dihydro-2(1H)-quinolinones, and oxindoles. Friedlander-type cyclization reactions provide a convenient route to various quinolines. Finally, cyclization reactions of amines with amines afford quinolines and phenylpyrrolidines.
机译:这篇综述总结了过去十年中基于过渡金属催化的氢转移反应的多种氮杂环合成方法。它们中的大多数使用铱和钌配合物作为催化剂,并提供了多种氮杂环化合物的通用且对环境无害的合成方法。胺与醇的分子间环化反应提供5-7元脂环族胺,喹啉,哌嗪,吲哚,喹喔啉,吡咯,苯并咪唑和苯并恶唑。氨基醇的分子内环化反应产生吲哚,1,2,3,4-四氢喹啉,1,2,3,4-四氢喹喔啉,3,4-二氢-2(1H)-喹啉酮和羟吲哚。弗里德兰德型环化反应提供了通往各种喹啉的便捷途径。最后,胺与胺的环化反应得到喹啉和苯基吡咯烷。

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